"Tekscan" T-Scan Occlusal analysis device & accessories (Non-Sterile)
Taiwan·Risk Class 1·MD·TEKSCAN, INC.·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- 84c83970e4058f589c3b420e8d5025e9
- License Form
- Ministry of Health Medical Device Import Registration No. 015516
- Customs Code
- DHA08401551604
- Manufacturer
- TEKSCAN, INC.
- Manufacturer Country
- United States
- Authorized Representative
- MEMS TECHNOLOGY CORP.
- Intended Use
- Limited to the first level recognition range of occlusal paper (F.6140) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6140 Occlusal paper
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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Access comprehensive regulatory information for "Tekscan" T-Scan Occlusal analysis device & accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 84c83970e4058f589c3b420e8d5025e9 and manufactured by TEKSCAN, INC.. The authorized representative in Taiwan is MEMS TECHNOLOGY CORP..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TEKSCAN, INC., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.